For practitioners
For people, by science.
LanFam Health was built from lived experience and refined with clinical precision — nutraceuticals and medical foods that bridge the gap between the clinic and daily life, where patients face the hardest work of recovery. Our process is grounded in human need, validated by evidence, standardized for consistency, and tested for safety, so you can recommend with confidence.
Grounded in human need
Built from lived experience — formulated around the problems patients actually bring into the clinic.
Validated by evidence
Every active earns its place through a defined, research-backed mechanism — not a trend.
Standardized for consistency
Botanicals and nutrients standardized to a verified potency, so the dose is the same every time.
Tested for safety
Identity, potency, contaminants, and allergens screened on every batch, cGMP in the USA.
01 — Active selection
Focused stacks, clear mechanisms.
We select botanicals, amino acids, and nutrients with defined roles — healthy inflammatory signaling, antioxidant support, neurotransmitter pathways, barrier integrity. Each active is standardized for dose consistency and verified by HPLC/UPLC assay. Open any card for its mechanism, dose, and the research behind it.
02 — Human evaluation
Measured change, never assumed.
Mechanisms matter, but outcomes are the test. ProleevaMax was evaluated in people, and the change was measured against a validated pain instrument.
McGill Pain Questionnaire
Mean reduction over an 8-week evaluation (p = 0.042) — both clinically meaningful and statistically significant.
03 — Testing & quality
Every batch verified.
Identity confirmed, potency measured, contaminants and allergens screened — so what you recommend is what reaches your patient.
Identity confirmed
Every active is assayed to confirm it is what the label says, by HPLC/UPLC.
Potency measured
Standardized extracts are quantified against their spec — not estimated.
Contaminants & allergens screened
Heavy metals, microbials, and common allergens tested out of every lot.
cGMP USA · COA per lot
Manufactured in cGMP-compliant US facilities. A Certificate of Analysis is available for every lot.
The 8-week evaluation describes ProleevaMax as formulated; it is a measured outcome, not a guarantee of individual results. Mechanism statements explain how each active is understood to work.
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.